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Variants search result for Homo sapiens
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32 records found for search term Rbm11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156268838CV2195042single nucleotide variantNM_144770.5(RBM11):c.6C>G (p.Phe2Leu)not specified [RCV004077960]uncertain significance211421619214216192Humanname
155939327CV2375744single nucleotide variantNM_144770.5(RBM11):c.13C>G (p.Gln5Glu)not specified [RCV004224339]uncertain significance211421619914216199Humanname
597708201CV3589721single nucleotide variantNM_144770.5(RBM11):c.98C>T (p.Ala33Val)not specified [RCV004860700]uncertain significance211421956414219564Humanname
156137408CV2210439single nucleotide variantNM_144770.5(RBM11):c.268C>T (p.Arg90Cys)not specified [RCV004089581]uncertain significance211422110514221105Humanname
401734775CV2690677single nucleotide variantNM_144770.5(RBM11):c.254G>A (p.Arg85Gln)not specified [RCV004298408]uncertain significance211421972014219720Humanname
405670134CV3308809single nucleotide variantNM_144770.5(RBM11):c.251A>G (p.Tyr84Cys)not specified [RCV004441090]uncertain significance211421971714219717Humanname
597784827CV3589720single nucleotide variantNM_144770.5(RBM11):c.221G>A (p.Arg74His)not specified [RCV004854575]uncertain significance211421968714219687Humanname
598252938CV3898623single nucleotide variantNM_144770.5(RBM11):c.244G>A (p.Val82Met)not specified [RCV005259504]uncertain significance211421971014219710Humanname
156397802CV2193735single nucleotide variantNM_144770.5(RBM11):c.385A>G (p.Ile129Val)not specified [RCV004074498]uncertain significance211422449014224490Humanname
156072477CV2267497single nucleotide variantNM_144770.5(RBM11):c.749A>G (p.Gln250Arg)not specified [RCV004135921]uncertain significance211422719614227196Humanname
156151851CV2318840single nucleotide variantNM_144770.5(RBM11):c.562A>G (p.Lys188Glu)not specified [RCV004175749]likely benign211422700914227009Humanname
156272722CV2323413single nucleotide variantNM_144770.5(RBM11):c.673G>A (p.Gly225Arg)not specified [RCV004171807]uncertain significance211422712014227120Humanname
156338080CV2343141single nucleotide variantNM_144770.5(RBM11):c.740G>A (p.Arg247Gln)not specified [RCV004194775]uncertain significance211422718714227187Humanname
329377414CV2435912single nucleotide variantNM_144770.5(RBM11):c.310A>G (p.Lys104Glu)not specified [RCV004255140]uncertain significance211422114714221147Humanname
329400541CV2438463single nucleotide variantNM_144770.5(RBM11):c.352G>A (p.Gly118Ser)not specified [RCV004259613]uncertain significance211422445714224457Humanname
401734732CV2709592single nucleotide variantNM_144770.5(RBM11):c.659C>T (p.Pro220Leu)not specified [RCV004318819]uncertain significance211422710614227106Humanname
401899885CV2755818single nucleotide variantNM_144770.5(RBM11):c.572A>G (p.His191Arg)not specified [RCV004342189]uncertain significance211422701914227019Humanname
401881804CV2774615single nucleotide variantNM_144770.5(RBM11):c.610G>C (p.Ala204Pro)not specified [RCV004350085]uncertain significance211422705714227057Humanname
405670142CV3308810single nucleotide variantNM_144770.5(RBM11):c.342A>T (p.Glu114Asp)not specified [RCV004441091]uncertain significance211422444714224447Humanname
405670147CV3308811single nucleotide variantNM_144770.5(RBM11):c.392A>C (p.Asn131Thr)not specified [RCV004441092]uncertain significance211422449714224497Humanname
405670151CV3308812single nucleotide variantNM_144770.5(RBM11):c.394A>T (p.Thr132Ser)not specified [RCV004441093]uncertain significance211422449914224499Humanname
405670157CV3308813single nucleotide variantNM_144770.5(RBM11):c.515C>A (p.Ser172Tyr)not specified [RCV004441094]uncertain significance211422696214226962Humanname
405670165CV3308815single nucleotide variantNM_144770.5(RBM11):c.595C>A (p.Leu199Ile)not specified [RCV004441096]uncertain significance211422704214227042Humanname
407467583CV3468831single nucleotide variantNM_144770.5(RBM11):c.602A>G (p.Gln201Arg)not specified [RCV004660761]uncertain significance211422704914227049Humanname
407467587CV3468832single nucleotide variantNM_144770.5(RBM11):c.803G>A (p.Cys268Tyr)not specified [RCV004660762]likely benign211422725014227250Humanname
407507327CV3468833single nucleotide variantNM_144770.5(RBM11):c.410A>G (p.Glu137Gly)not specified [RCV004671683]uncertain significance211422451514224515Humanname
597708212CV3589722single nucleotide variantNM_144770.5(RBM11):c.634G>A (p.Val212Met)not specified [RCV004860701]uncertain significance211422708114227081Humanname
597784835CV3589724single nucleotide variantNM_144770.5(RBM11):c.638C>T (p.Ser213Phe)not specified [RCV004854577]uncertain significance211422708514227085Humanname
597708221CV3589725single nucleotide variantNM_144770.5(RBM11):c.628G>A (p.Ala210Thr)not specified [RCV004860702]likely benign211422707514227075Humanname
597708233CV3589726single nucleotide variantNM_144770.5(RBM11):c.568A>G (p.Thr190Ala)not specified [RCV004860703]uncertain significance211422701514227015Humanname
598252943CV3898624single nucleotide variantNM_144770.5(RBM11):c.802T>C (p.Cys268Arg)not specified [RCV005259505]uncertain significance211422724914227249Humanname
598252955CV3898626single nucleotide variantNM_144770.5(RBM11):c.626G>C (p.Ser209Thr)not specified [RCV005259507]uncertain significance211422707314227073Humanname